…nd family history matter. Many common variants do not cause disease.
Nutrients and next steps
A genetic finding cannot show a nutrient deficiency or tell you how much of a supplement to take. Bring the original report to your clinician and …
…receptor system involved in uptake of the intrinsic-factor–B12 complex.
Also called: Cubilin
Start here
Encodes cubilin, part of a receptor system involved in uptake of the intrinsic-factor–B12 complex.
How this gene connects
You may see CU…
…nd family history matter. Many common variants do not cause disease.
Nutrients and next steps
A genetic finding cannot show a nutrient deficiency or tell you how much of a supplement to take. Bring the original report to your clinician and …
DIO1 is the gene name for Deiodinase, Iodothyronine Type I. Learn what a specific result could mean and what to ask about it.
Also called: Deiodinase, Iodothyronine Type I
Start here
DIO1 is the gene name for Deiodinase, Iodothyronine Type …
…nd family history matter. Many common variants do not cause disease.
Nutrients and next steps
A genetic finding cannot show a nutrient deficiency or tell you how much of a supplement to take. Bring the original report to your clinician and …
…nd family history matter. Many common variants do not cause disease.
Nutrients and next steps
A genetic finding cannot show a nutrient deficiency or tell you how much of a supplement to take. Bring the original report to your clinician and …
…rolling how other genes are used. You may see the label GABP1 in older materials; check the exact variant on your own report.
Also called: GABP1, GA Binding Protein Transcription Factor Subunit Alpha
Start here
GABPA is a gene involved in c…
…nd family history matter. Many common variants do not cause disease.
Nutrients and next steps
A genetic finding cannot show a nutrient deficiency or tell you how much of a supplement to take. Bring the original report to your clinician and …
…nd family history matter. Many common variants do not cause disease.
Nutrients and next steps
A genetic finding cannot show a nutrient deficiency or tell you how much of a supplement to take. Bring the original report to your clinician and …
KCTD10 is the gene name for Potassium Channel Tetramerization Domain Containing 10. Learn what a specific result could mean and what to ask about it.
Also called: Potassium Channel Tetramerization Domain Containing 10
Start here
KCTD10 is t…
…nd family history matter. Many common variants do not cause disease.
Nutrients and next steps
A genetic finding cannot show a nutrient deficiency or tell you how much of a supplement to take. Bring the original report to your clinician and …
…nd family history matter. Many common variants do not cause disease.
Nutrients and next steps
A genetic finding cannot show a nutrient deficiency or tell you how much of a supplement to take. Bring the original report to your clinician and …
Search looks for your words in titles, descriptions, available articles, learning guides, and video captions when available. The closest matches appear first. Duplicate posts are grouped, with links to other places you can read or watch them. Books, chapters, and reports have topic guides here; the original files and full book text are not available in this encyclopedia. Subscriber posts include a title and public summary; open Substack to read the full post.